Australia - English - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - tramadol hydrochloride, quantity: 37.5 mg; paracetamol, quantity: 325 mg - tablet, film coated - excipient ingredients: microcrystalline cellulose; stearic acid; hyprolose; croscarmellose sodium; titanium dioxide; iron oxide yellow; macrogol 8000; hypromellose; povidone; pregelatinised maize starch - tramadol/paracetamol is indicated for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.

Australia - English - Department of Health (Therapeutic Goods Administration)

aspen pharmacare australia pty ltd - tramadol hydrochloride, quantity: 37.5 mg; paracetamol, quantity: 325 mg - tablet, effervescent - excipient ingredients: povidone; sunset yellow fcf; saccharin sodium; citric acid; sodium bicarbonate; macrogol 6000; acesulfame potassium; sodium dihydrogen citrate; colloidal anhydrous silica; magnesium stearate; flavour - zaldiar is indicated for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.

Australia - English - Department of Health (Therapeutic Goods Administration)

aspen pharmacare australia pty ltd - paracetamol, quantity: 325 mg; tramadol hydrochloride, quantity: 37.5 mg - tablet, film coated - excipient ingredients: powdered cellulose; magnesium stearate; macrogol 6000; sodium starch glycollate type a; titanium dioxide; hypromellose; pregelatinised maize starch; purified talc; iron oxide yellow; lactose monohydrate; maize starch; propylene glycol - zaldiar is indicated for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.

Australia - English - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - tramadol hydrochloride, quantity: 37.5 mg; paracetamol, quantity: 325 mg - tablet, film coated - excipient ingredients: microcrystalline cellulose; macrogol 8000; hypromellose; hyprolose; stearic acid; titanium dioxide; croscarmellose sodium; iron oxide yellow; pregelatinised maize starch; povidone - tramadol/paracetamol is indicated for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.

Ireland - English - HPRA (Health Products Regulatory Authority)

mcdermott laboratories ltd., t/a gerard laboratories - tramadol hydrochloride; paracetamol - film-coated tablet - 37.5 mg/325 milligram(s) - opioids in combination with non-opioid analgesics; opiods in combination with non-opiod analgesics

Ireland - English - HPRA (Health Products Regulatory Authority)

athlone laboratories ltd - paracetamol; tramadol hydrochloride - film-coated tablet - 37.5/325 milligram(s) - other opioids; tramadol, combinations

Ireland - English - HPRA (Health Products Regulatory Authority)

generics (uk) limited - tramadol hydrochloride; paracetamol 90% dcl (compap l) - film-coated tablet - 37.5/325 milligram(s) - opioids in combination with non-opioid analgesics; opiods in combination with non-opiod analgesics

Ireland - English - HPRA (Health Products Regulatory Authority)

athlone pharmaceuticals limited - tramadol hydrochloride; paracetamol - film-coated tablet - other opioids; tramadol, combinations

United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

krka uk ltd - paracetamol; tramadol hydrochloride - oral tablet - 325mg ; 37.5mg

United States - English - NLM (National Library of Medicine)

rebel distributors corp. - tramadol hydrochloride (unii: 9n7r477wck) (tramadol - unii:39j1lgj30j) - tramadol hydrochloride 100 mg - tramadol hydrochloride er tablets are indicated for the management of moderate to moderately severe chronic pain in adults who require around-the-clock treatment of their pain for an extended period of time. tramadol hydrochloride er tablets should not be administered to patients who have previously demonstrated hypersensitivity to tramadol, any other component of this product or opioids. tramadol hydrochloride er tablets are contraindicated in any situation where opioids are contraindicated, including acute intoxication with any of the following: alcohol, hypnotics, narcotics, centrally acting analgesics, opioids or psychotropic drugs. tramadol hydrochloride er tablets may worsen central nervous system and respiratory depression in these patients tramadol hydrochloride is a mu-agonist opioid. tramadol, like other opioids used in analgesia, can be abused and is subject to criminal diversion. drug addiction is characterized by compulsive use, use for non-medical purposes, and continued use despite harm or risk